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Interactions equation

It must be remembered that, in general, the constants a and b of the van der Waals equation depend on volume and on temperature. Thus a number of variants are possible, and some of these and the corresponding adsorption isotherms are given in Table XVII-2. All of them lead to rather complex adsorption equations, but the general appearance of the family of isotherms from any one of them is as illustrated in Fig. XVII-11. The dotted line in the figure represents the presumed actual course of that particular isotherm and corresponds to a two-dimensional condensation from gas to liquid. Notice the general similarity to the plots of the Langmuir plus the lateral interaction equation shown in Fig. XVII-4. [Pg.624]

Here we consider the total interaction between two charged particles in suspension, surrounded by tlieir counterions and added electrolyte. This is tire celebrated DLVO tlieory, derived independently by Derjaguin and Landau and by Verwey and Overbeek [44]. By combining tlie van der Waals interaction (equation (02.6.4)) witli tlie repulsion due to the electric double layers (equation (C2.6.lOI), we obtain... [Pg.2681]

The energy of solvation can be further broken down into terms that are a function of the bulk solvent and terms that are specifically associated with the first solvation shell. The bulk solvent contribution is primarily the result of dielectric shielding of electrostatic charge interactions. In the simplest form, this can be included in electrostatic interactions by including a dielectric constant k, as in the following Coulombic interaction equation ... [Pg.206]

HyperChem also provides a shifting potential for terminating nonbonded interactions (equation 15). [Pg.30]

Interaction Representation.—In many physical problems the hamiltonian of a system that is engaged in interaction with another is of the form H + V,H being the stationary normal ( unperturbed ) hamiltonian and V the interaction. Equation (7-51) then reads... [Pg.418]

Since the gravitational constant is extremely small, it is natural to expect that the force of interaction is also very small too. For illustration, consider two spheres with radius Im and mass 31.4x10 kg made from galena, with the distance between their centers 10 m. Then, the force of interaction, Equation (1.1), is... [Pg.3]

Compartmental soil modeling is a new concept and can apply to both modules. For the solute fate module, for example, it consists of the application of the law of pollutant mass conservation to a representative user specified soil element. The mass conservation principle is applied over a specific time step, either to the entire soil matrix or to the subelements of the matrix such as the soil-solids, the soil-moisture and the soil-air. These phases can be assumed in equilibrium at all times thus once the concentration in one phase is known, the concentration in the other phases can be calculated. Single or multiple soil compartments can be considered whereas phases and subcompartments can be interrelated (Figure 2) with transport, transformation and interactive equations. [Pg.53]

Equations (18) and (16) define a temperature where Gaussian behavior is observed (the phase separation temperature) where % — 1/2 and thermal energy is just sufficient to break apart PP and SS interactions to form PS interactions. Equation (12) using (17) for Vc is called the Flory-Krigbaum equation. This expression indicates that only three states are possible for a polymer coil at thermal equilibrium ... [Pg.129]

An interaction equation, based on criteria from AHCE Manual 42 can be applied to determine acceptable behavior ... [Pg.190]

Next, predictive equations for activity coefficients in mixed electrolyte solutions, based upon results in simpler ones, will be mentioned. The work of Brjlnsted (12) and of Guggenheim (13) led to the specific interaction equation... [Pg.566]

Since l is proportional to and q is proportional to 1/L, i is proportional to. Substitution of Eq. (67) into Eq.(62) gives the Langevin equation for the Rouse modes of the chain within the approximations of preaveraging for hydrodynamic interactions and mode-mode decoupling for intersegment potential interactions. Equation (62) yields the following results for relaxation times and various dynamical correlation functions. [Pg.15]

F. 1.2.2 The resultant applied force (FRS/, FRDp and the resultant applied moment MRSp, MRDp) acting on each pump nozzle flange shall satisfy the appropriate interaction equation (Equations F-1 and F-2). [Pg.119]

FIGURE 2. Calculated powder patterns for spin-1 (a) and spin-3/2 (b) nuclei with a dominating quadrupolar interaction (QUASAR simulation) tj is the asymmetry parameter of the quadmpolar interaction (equation (9))... [Pg.142]

The loads acting on each nozzle satisfy the appropriate interaction equation, so the condition specified in F.1.2 b is satisfied. [Pg.131]

Not only heteroatoms but also double bonds can be used as chelating groups via -interaction (equation 39)49. [Pg.620]

It should be apparent that the expressions for the wave functions after interaction [equations (3.38) and (3.39)] are equivalent to the Rayleigh-Schrodinger perturbation theory (RSPT) result for the perturbed wave function correct to first order [equation (A.109)]. Similarly, the parallel between the MO energies [equations (3.33) and (3.34)] and the RSPT energy correct to second order [equation (A. 110)] is obvious. The missing first-order correction emphasizes the correspondence of the first-order corrected wave function and the second-order corrected energy. Note that equations (3.33), (3.34), (3.38), and (3.39) are valid under the same conditions required for the application of perturbation theory, namely that the perturbation be weak compared to energy differences. [Pg.45]

Our kinetic model in this case corresponds to the Ising model with symmetrical nearest-neighbor interactions. Equation (4) is consistent with the result of detailed balancing when applied to each pair of elementary steps in scheme I. The solution for the experimentally most important quantities... [Pg.284]

Incorporation of the reactant interaction, equations (2.3.47) to (2.3.50), leads to the non-linear equations, both in Y(r, t) and in nA(t) and nB(t). Non-linear terms arise due to the integral terms in equation (2.3.50) describing the effective interaction of particles with their environment. The linearization of this equation, justified if the concentrations are small, yields... [Pg.175]

Making use of the elastic constant entering equation (3.1.4) for F, H centres in KBr a = 3 eVA3 [69], one can estimate easily that the effective radius of annihilation stimulated by elastic interaction, (equation (4.2.29)) varies... [Pg.204]


See other pages where Interactions equation is mentioned: [Pg.221]    [Pg.2184]    [Pg.227]    [Pg.845]    [Pg.175]    [Pg.302]    [Pg.149]    [Pg.128]    [Pg.42]    [Pg.123]    [Pg.82]    [Pg.420]    [Pg.748]    [Pg.896]    [Pg.85]    [Pg.88]    [Pg.571]    [Pg.21]    [Pg.259]    [Pg.63]    [Pg.109]    [Pg.126]    [Pg.154]    [Pg.929]    [Pg.184]    [Pg.199]   
See also in sourсe #XX -- [ Pg.79 ]




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Derivation of nuclear spin interactions from the Breit equation

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Equation Relativistic configuration interaction

Equations for Solid—Solution Interactions

Equations, mathematical dispersion interaction

Equations, mathematical interaction

Flory-Huggins equations interaction parameter

Hartree-Fock equations/theory configuration interaction

Interaction site fluids integral equation solutions

Magnetic-interaction constants, defining equations

ORBITAL INTERACTION THEORY Relationship to Hartree-Fock Equations

Poisson-Boltzmann equation polyelectrolyte-counterion interactions

RISM integral equation, solute-solvent interactions

Reference interaction-site model integral equation

Response equations interaction wave functions

Schrodinger equation interaction representation

Solid-solution interactions equations

Specific interaction equations

Specific interaction equations models

The specific ion interaction equations

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